ENST00000274547.7:c.1022C>T
|
ENSP00000274547.2:p.Ala341Val
|
|
ENST00000393959.6:c.1022C>T
MANE Select
|
ENSP00000377531.1:p.Ala341Val
|
|
ENST00000674514.1:n.1104C>T
|
|
|
ENST00000675081.1:c.*481C>T
|
ENSP00000502207.1:n.*481C>T
|
|
ENST00000675303.1:c.1022C>T
|
ENSP00000502748.1:p.Ala341Val
|
|
ENST00000675381.1:c.770C>T
|
ENSP00000501968.1:p.Ala257Val
|
|
ENST00000675746.1:c.272C>T
|
ENSP00000502391.1:p.Ala91Val
|
|
ENST00000675773.1:c.1022C>T
|
ENSP00000502701.1:p.Ala341Val
|
|
ENST00000274547.6:c.1022C>T
|
ENSP00000274547.2:p.Ala341Val
|
|
ENST00000353437.10:c.1022C>T
|
ENSP00000274546.6:p.Ala341Val
|
|
ENST00000393959.5:c.1022C>T
|
ENSP00000377531.1:p.Ala341Val
|
|
ENST00000517547.5:c.542C>T
|
ENSP00000429750.1:p.Ala181Val
|
|
ENST00000517901.5:c.833C>T
|
ENSP00000430532.1:p.Ala278Val
|
|
ENST00000520240.5:c.1022C>T
|
ENSP00000429320.1:p.Ala341Val
|
|
ENST00000612710.1:c.833C>T
|
ENSP00000480066.1:p.Ala278Val
|
|
NM_000813.2:c.1022C>T
|
NP_000804.1:p.Ala341Val
|
|
NM_021911.2:c.1022C>T
|
NP_068711.1:p.Ala341Val
|
|
XM_011534501.1:c.272C>T
|
XP_011532803.1:p.Ala91Val
|
|
NM_000813.3:c.1022C>T
|
NP_000804.1:p.Ala341Val
|
|
NM_001371727.1:c.1022C>T
MANE Select
|
NP_001358656.1:p.Ala341Val
|
|
NM_021911.3:c.1022C>T
|
NP_068711.1:p.Ala341Val
|
|